FDA UDI In Commercial Distribution 🇺🇸 United States

N/A (Approved Vendor)

DI: 10194484321632 · Model: 21F229 · GRAINGER INTERNATIONAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1000

Basic Information

Brand Name
N/A (Approved Vendor)
Primary DI
10194484321632
Version / Model
21F229
Company Name
GRAINGER INTERNATIONAL, INC.
Labeler DUNS
053618240
Distribution Status
In Commercial Distribution
Device Count in Pkg
1000
Record Status
Published
Publish Date
2025-08-11
Public Version
1
Public Version Date
2025-08-19
Public Version Status
New
Public Device Record Key
83680cec-17a8-4cf7-95af-44b6f32ad984

Device Description

Pipette Transfer,1.5mL,PK1000

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GJW Pipette, Pasteur

GMDN Terms

Code Name
64876 Specimen transfer scooping tool IVD

Identifiers

Type ID
Package 20194484321639
Primary 10194484321632
Unit of Use 00194484321635